US8003101B2ExpiredUtilityA1
Inflammatory mediator antagonists
Est. expiryMar 26, 2018(expired)· nominal 20-yr term from priority
A61P 43/00A61P 37/02A61P 37/06A61P 29/00A61P 25/00A61P 25/28A61P 19/02A61P 19/04A61P 11/00A61P 1/04A61P 11/06A61P 17/06A61K 45/06C07K 16/248A61K 31/519C07K 2317/76C07K 2319/00C07K 14/52A61K 2039/505C07K 2319/30A61K 31/00C07K 16/24C07K 14/7155A61K 39/395
79
PatentIndex Score
7
Cited by
133
References
9
Claims
Abstract
The present invention relates to methods of reducing cartilage degradation in a patient comprising administering to a patient in need thereof an effective amount of an antibody antagonist to the mature form of OSM.
Claims
exact text as granted — not AI-modified1. A method of reducing cartilage degradation in a patient comprising administering to a patient in need thereof an effective amount of an anti-OSM antagonist antibody to the mature form of SEQ ID NO:12, wherein said antibody reduces the TNFα secretion from macrophages in said patient and interacts with at least one of the residues selected from the group consisting of: G120, Q16, Q20, N123 and N124 of the mature form of SEQ ID NO:12.
2. The method of claim 1 wherein said patient suffers from an inflammatory disorder selected from the group consisting of: rheumatoid arthritis, psoriatic arthritis, juvenile arthritis, inflammatory osteoarthritis, reactive arthritis, Crohns disease, ulcerative colitis, gastritis, asthma, chronic obstructive pulmonary disease, Alzheimer's disease, multiple sclerosis and psoriasis.
3. The method according to claim 1 , wherein the anti-OSM antagonist antibody is an antibody of the receptor gp130 (type II) of human oncostatin M as set forth in the mature form of SEQ ID NO:12.
4. The method according to claim 1 wherein the antibody is humanized or chimerized.
5. The method according to claim 1 , wherein the anti-OSM antagonist antibody further prevents or reduces collagen release from cartilage.
6. The method according to claim 2 wherein said disorder is rheumatoid arthritis.
7. The method of claim 1 wherein the antibody is administered alone.
8. The method of claim 1 wherein the antibody is administered in combination with an immunosuppressive agent.
9. The method of claim 1 wherein the antibody is administered subcutaneously.Join the waitlist — get patent alerts
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